NA 0502990070Recalls & reported problems
Stryker Corporation · Cystoscope, Autoclavable, 70 ¿ View Direction · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327063998), received between Dec 2, 2019 and Mar 2, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fogging” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fogging1
- No Display/Image1
- Optical Distortion1
- Optical Obstruction1
- Optical Problem1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 2, 2026Fogging; Optical Distortion
IT WAS REPORTED THAT THE SCOPE WAS CLOUDY.
Patient problems: Insufficient Information
MAUDE report 24491378 ↗MalfunctionJun 1, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS LACK OF IMAGE DURING PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17040717 ↗MalfunctionDec 2, 2019Optical Obstruction; No Display/Image; Optical Obstruction
IT WAS REPORTED THAT THERE COULD BE A POTENTIAL OF ADVERSE CONSEQUENCES DUE TO IMAGE LOSS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9398930 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.